FDA UDI In Commercial Distribution 🇺🇸 United States

QDOT MICRO

DI: 10846835017076 · Model: D139402 · Biosense Webster Inc
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
QDOT MICRO
Primary DI
10846835017076
Version / Model
D139402
Catalog Number
D139402
Company Name
Biosense Webster Inc
Labeler DUNS
020163218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-07
Public Version
1
Public Version Date
2023-07-17
Public Version Status
New
Public Device Record Key
2edf354e-e44b-460b-a93b-7892cfa6bd5b

Device Description

Uni-Directional Navigation Catheter, NAV, F

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OAE Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation
OAD catheter, percutaneous, cardiac ablation, for treatment of atrial flutter

GMDN Terms

Code Name
61785 Cardiac radio-frequency ablation system catheter

Identifiers

Type ID
Primary 10846835017076

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Storage Environment Temperature
Temperature Range
41 – 77 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damaged
Type
Storage Environment Temperature
Temperature Range
5 – 25 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Do not use if use if box is opened